drugset / Trial / NCT07450495
Effect of Different Concentrations of Sevoflurane for Anesthesia Induction in Pediatric Ophthalmic Surgery
Recruiting
80 enrolled
Joint Shantou International Eye Center of Shantou University and the Chinese University of Hong Kong
RandomizedParallel-groupSingle-blindTreatment
Summary
This randomized controlled trial aims to compare the effectiveness and safety of 6% versus 8% sevoflurane inhalation induction in pediatric patients undergoing minor ophthalmic surgery. The primary outcome is emergence agitation assessed using the Pediatric Anesthesia Emergence Delirium (PAED) scale. Secondary outcomes include hemodynamic parameters, induction time, recovery time, and adverse events.
Timeline
- Start
- 2025-02-25
- Primary completion
- 2026-02-25
- Completion
- 2026-04-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Sevoflurane | Other / unclassified | 6 % | Inhaled |
| Subject | Sevoflurane | Other / unclassified | 8 % | Inhaled |